<p>(A) Lateral views of wild type, single or double mutant mouse embryos of indicated genotype at E14.5. Exencephaly is apparent in the <i>Tctn1</i><sup>-/-</sup><i>Nphp1</i><sup>-/-</sup> double mutant. Corresponding Alcian blue staining of the right forelimb (top) and hindlimb (bottom) are included, with asterisks indicating extra digits. Genes encoding components of the NPHP complex are indicated in red. Genes encoding components of the MKS complex are indicated in green. Scale bars, 1 mm. (B) Number of digits in the forelimbs and (C) hindlimbs of wild type, single or double mutant embryos of indicated genotypes. (D) Incidence of exencephaly in wild type, single or double mutants embryos of indicated genotypes. Numbers of animals analyze...
Congenital abnormalities can be modeled in the mouse using genetic approaches such as phenotype driv...
Understanding the mechanisms that lead to axial elongation in the mouse has direct relevance to eluc...
In multigenic diseases, disorders where mutations in multiple genes affect the expressivity of the d...
<p>(A) Lateral views of wild type, <i>Tctn1</i><sup>-/-</sup>, <i>Bbs1</i><sup>-/-</sup> and <i>Tctn...
Background: Identifying genes that are essential for mouse embryonic development and survival throug...
The SELH/Bc mouse strain, a model for multifactorial human neural tube defects, has 10-30% exencepha...
This project was the first study of the genetics and embryo-pathology of exencephaly in a partially ...
<p>(A) The gene targeting strategy used to create mouse <i>Cep120<sup>-</sup></i> and <i>Cep120<sup>...
BACKGROUND: Mutagenesis screens in the mouse have been proven useful for the identification of novel...
<p>(A) Limb bud sections (left) from E11.5 embryos were stained for acetylated tubulin (Tub<sup>Ac</...
Analysis of the embryonic phenotype of Bent tail, a mouse model for X-linked neural tube defects.Fra...
AbstractWe describe a novel transgene insertional mouse mutant with skeletal abnormalities character...
Kooistra MK, Leduc RYM, Dawe CE, Fairbridge NA, Rasmussen J, Man JHY, Bujold M, Juriloff D, King-Jon...
BACKGROUND: Mutagenesis screens in the mouse have been proven useful for the identification of novel...
Item does not contain fulltextNeural tube defects, mostly believed to result from closure defects of...
Congenital abnormalities can be modeled in the mouse using genetic approaches such as phenotype driv...
Understanding the mechanisms that lead to axial elongation in the mouse has direct relevance to eluc...
In multigenic diseases, disorders where mutations in multiple genes affect the expressivity of the d...
<p>(A) Lateral views of wild type, <i>Tctn1</i><sup>-/-</sup>, <i>Bbs1</i><sup>-/-</sup> and <i>Tctn...
Background: Identifying genes that are essential for mouse embryonic development and survival throug...
The SELH/Bc mouse strain, a model for multifactorial human neural tube defects, has 10-30% exencepha...
This project was the first study of the genetics and embryo-pathology of exencephaly in a partially ...
<p>(A) The gene targeting strategy used to create mouse <i>Cep120<sup>-</sup></i> and <i>Cep120<sup>...
BACKGROUND: Mutagenesis screens in the mouse have been proven useful for the identification of novel...
<p>(A) Limb bud sections (left) from E11.5 embryos were stained for acetylated tubulin (Tub<sup>Ac</...
Analysis of the embryonic phenotype of Bent tail, a mouse model for X-linked neural tube defects.Fra...
AbstractWe describe a novel transgene insertional mouse mutant with skeletal abnormalities character...
Kooistra MK, Leduc RYM, Dawe CE, Fairbridge NA, Rasmussen J, Man JHY, Bujold M, Juriloff D, King-Jon...
BACKGROUND: Mutagenesis screens in the mouse have been proven useful for the identification of novel...
Item does not contain fulltextNeural tube defects, mostly believed to result from closure defects of...
Congenital abnormalities can be modeled in the mouse using genetic approaches such as phenotype driv...
Understanding the mechanisms that lead to axial elongation in the mouse has direct relevance to eluc...
In multigenic diseases, disorders where mutations in multiple genes affect the expressivity of the d...